K260931
- 510(k) number
- K260931
- Device name
- Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R)
- Applicant
- Unimed Medical Supplies, Inc. CN
- Product code
- DQA — Oximeter
- Decision date
- 2026-04-14
- Date received
- 2026-03-20
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K260931.pdf
Official FDA record: K260931
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.